Canonical Allele Identifier: CA1190289488
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709609T= , CM000663.2:g.114709609T= GRCh38
NC_000001.10:g.115252230T= , CM000663.1:g.115252230T= GRCh37
NC_000001.9:g.115053753T= NCBI36
NG_007572.1:g.12286A= , LRG_92:g.12286A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.410A= MANE Select ENSP00000358548.4:p.Tyr137=
ENST00000369535.4:c.410A= ENSP00000358548.4:p.Tyr137=
NM_002524.4:c.410A= NP_002515.1:p.Tyr137=
NM_002524.5:c.410A= MANE Select NP_002515.1:p.Tyr137=